About: Synthesis of Cyclopropanes via Pd(II/IV)-Catalyzed Reactions of Enynes

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scientific article published on 14 April 2007

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в травні 2007 (uk) article scientifique publié en 2007 (fr) im Mai 2007 veröffentlichter wissenschaftlicher Artikel (de) scientific article published on 14 April 2007 (en) artículu científicu espublizáu n'abril de 2007 (ast)
publication date	wds:Q57944565-DD74AA86-9F9C-4CDD-ADA7-8A578615E33D
publication date	2007-04-14 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q57944565-4B55F81D-7D4A-4F8F-A064-4A5A55CACF13
language of work or name	English
cites work	wds:Q57944565-FD90CB61-A549-4377-9B17-C08CDD0D6453
cites work	New catalytic methods for the synthesis of selectively substituted aromatics through palladacycles
author name string	wds:Q57944565-3C89D01B-157F-42D6-A562-C9D40CF398EF wds:Q57944565-41F1E6BF-7470-4CF9-9F65-083591932953 wds:Q57944565-5775498A-5894-429E-B9D6-2EC3E7114BF3
author name string	Thomas W Lyons Leilani L Welbes Katie A Cychosz
rdfs:label	Synthesis of Cyclopropanes via Pd (nl) Synthesis of Cyclopropanes via Pd(II/IV)-Catalyzed Reactions of Enynes (en)
skos:prefLabel	Synthesis of Cyclopropanes via Pd (nl) Synthesis of Cyclopropanes via Pd(II/IV)-Catalyzed Reactions of Enynes (en)
name	Synthesis of Cyclopropanes via Pd (nl) Synthesis of Cyclopropanes via Pd(II/IV)-Catalyzed Reactions of Enynes (en)
author	wds:Q57944565-805CEB9E-1B0C-46B1-BE0B-C25FD446F390
author	Melanie S. Sanford
title	wds:Q57944565-623E21A8-A765-4003-B609-1EFDE8544DFB
title	Synthesis of cyclopropanes via Pd(II/IV)-catalyzed reactions of enynes (en)
page(s)	wds:Q57944565-D60BEE66-C54B-4234-9099-ADD9ACE503A0
page(s)	5836-5837
instance of	wds:Q57944565-0149387C-74A4-4755-9168-266BAB432FE9
instance of	scholarly article
PubMed ID	wds:Q57944565-CAB64482-4649-4CAE-B7A7-924B60119E75
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/17432861
PubMed ID	17432861
published in	wds:Q57944565-98A8F948-D869-4C2E-B921-0F1FBAFFA3D8
published in	Journal of the American Chemical Society
issue	wds:Q57944565-36D03BA3-BAEF-47A4-ADDE-B00DEA89DCCA
volume	wds:Q57944565-6EC1D031-B37D-4235-AA35-81B369DFCB1A
issue	18
volume	129
DOI	wds:Q57944565-3D7FA3CA-4181-4061-AC09-53DDAB88465B
DOI	http://dx.doi.org/10.1021/JA071204J
DOI	10.1021/JA071204J
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q57944565
is cites work of	Organopalladium(IV) chemistry Mechanistic approaches to palladium-catalyzed alkene difunctionalization reactions Chemistry of polyvalent iodine Advancing the mechanistic understanding of an enantioselective palladium-catalyzed alkene difunctionalization reaction Palladium(II)-catalyzed alkene functionalization via nucleopalladation: stereochemical pathways and enantioselective catalytic applications. Intercepting Wacker intermediates with arenes: C-H functionalization and dearomatization Synthetic and mechanistic studies of Pd-catalyzed C-H arylation with diaryliodonium salts: evidence for a bimetallic high oxidation state Pd intermediate Pd(II)-catalyzed oxidative 1,1-diarylation of terminal olefins Asymmetric chiral ligand-directed alkene dioxygenation Bystanding F+ oxidants enable selective reductive elimination from high-valent metal centers in catalysis On the mechanism of palladium-catalyzed aromatic C-H oxidation A gold(I)-catalyzed intramolecular oxidation-cyclopropanation sequence of 1,6-enynes: a convenient access to [n.1.0]bicycloalkanes. Palladium-catalyzed 1,1-aryloxygenation of terminal olefins Palladium-catalyzed oxidative carbocyclizations Asymmetric intramolecular α-cyclopropanation of aldehydes using a donor/acceptor carbene mimetic. Palladium (II/IV) catalyzed cyclopropanation reactions: scope and mechanism Palladium-catalyzed aerobic (1+2) annulation of Csp3-H bonds with olefin for the synthesis of 3-azabicyclo[3.1.0]hex-2-ene. A thiocyanopalladation/carbocyclization transformation identified through enzymatic screening: stereocontrolled tandem C-SCN and C-C bond formation. Palladium-Catalyzed Tunable Functionalization of Allylic Imidates: Regioselective Aminodiacetoxylation and Aziridination Palladium-catalyzed cascade annulation to construct functionalized β- and γ-lactones in ionic liquids. Extending the Salinilactone Family Palladium(II)-catalyzed enantio- and diastereoselective synthesis of pyrrolidine derivatives Recent progress towards transition metal-catalyzed synthesis of γ-lactams Efficient synthesis of substituted 3-azabicyclo[3.1.0]hexan-2-ones from 2-iodocyclopropanecarboxamides using a copper-free Sonogashira coupling Au(I)-catalyzed intramolecular oxidative cyclopropanation of 1,6-enynes derived from propiolamides with diphenyl sulfoxide The carbomethylation of arylacrylamides leading to 3-ethyl-3-substituted indolin-2-one by cascade radical addition/cyclization. Hypervalent Iodine Reagents in High Valent Transition Metal Chemistry. Anti-Markovnikov hydroalkylation of allylic amine derivatives via a palladium-catalyzed reductive cross-coupling reaction Structural Elucidation of Trace Components Combining GC/MS, GC/IR, DFT-Calculation and Synthesis-Salinilactones, Unprecedented Bicyclic Lactones from Salinispora Bacteria Synthesis of fused N-heterocycles via tandem C-H activation. Palladium-catalyzed oxidative arylacetoxylation of alkenes: synthesis of indole and indoline derivatives. One-Pot Synthesis of Cyclopropane-Fused Cyclic Amidines: An Oxidative Carbanion Cyclization. Construction of Polycyclic γ-Lactams and Related Heterocycles via Electron Catalysis. Pd-Catalyzed oxidative isomerization of propargylic acetates: highly efficient access to α-acetoxyenones via alkenyl Csp(2)-O bond-forming reductive elimination from Pd(IV). Palladium-catalyzed oxidative 6-exo-trig cyclization of 1,6-enynes: facile synthesis of bicyclo[4.1.0]heptan-5-ones.
is cites work of	wds:Q37683501-333227C3-DA0D-4791-99B8-DA70F490D65B wds:Q43066983-218BA752-F811-4D25-B488-31578A0289F1 wds:Q42544426-E1CB0CDC-F33E-4359-A685-D732954B1E0E wds:Q48275055-053CFAB4-758B-4901-B7EA-E67CA92408AA wds:Q57834065-2237589E-0220-4D74-B4FE-765E8B2179A9 wds:Q36282903-6EDBF2D9-4771-468D-8C88-2AE7271752D5 wds:Q42209953-F788E401-4D49-4AD9-994B-0FB3EA5911EB wds:Q46482980-CC68B569-89B9-4143-B091-AD5CBDAD3C70 wds:Q42644956-DF708641-D1E2-4D0D-A1A2-118175E5FEA1 wds:Q49686840-2659163C-85A7-4889-8FB1-45A24E1A5420 wds:Q48103825-5B66A03F-9608-48A2-B5C6-A36D7710F4D1 wds:Q39302515-1EF414AD-32F2-4A00-BBA2-2CAF0DE6E70B wds:Q39734585-00F155B3-6395-4D40-A4B2-78E9C3E4E686 wds:Q50455721-1A997B35-0370-40DF-882D-BA098379E789 wds:Q53607793-88FFA5F4-2297-4AA5-BF49-3810C0C306A2 wds:Q52641525-6DFD09B1-1D7B-4AE7-A000-20DBBB67F00C wds:Q34733581-584FB01D-BC97-46EC-8D1C-90170B4F3651 wds:Q42090053-B88FA72B-2C6F-40D8-8BA0-7ECB3B52C3BB wds:Q50512826-D262EC5C-7ED0-40BE-BAAC-F75E00D33B83

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